These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

151 related articles for article (PubMed ID: 30203597)

  • 1. Perlecan/HSPG2: Signaling role of domain IV in chondrocyte clustering with implications for Schwartz-Jampel Syndrome.
    Martinez JR; Grindel BJ; Hubka KM; Dodge GR; Farach-Carson MC
    J Cell Biochem; 2019 Feb; 120(2):2138-2150. PubMed ID: 30203597
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Perlecan is required for the chondrogenic differentiation of synovial mesenchymal cells through regulation of Sox9 gene expression.
    Sadatsuki R; Kaneko H; Kinoshita M; Futami I; Nonaka R; Culley KL; Otero M; Hada S; Goldring MB; Yamada Y; Kaneko K; Arikawa-Hirasawa E; Ishijima M
    J Orthop Res; 2017 Apr; 35(4):837-846. PubMed ID: 27238423
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Perlecan, A Multi-Functional, Cell-Instructive, Matrix-Stabilizing Proteoglycan With Roles in Tissue Development Has Relevance to Connective Tissue Repair and Regeneration.
    Hayes AJ; Farrugia BL; Biose IJ; Bix GJ; Melrose J
    Front Cell Dev Biol; 2022; 10():856261. PubMed ID: 35433700
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Ablation of Perlecan Domain 1 Heparan Sulfate Reduces Progressive Cartilage Degradation, Synovitis, and Osteophyte Size in a Preclinical Model of Posttraumatic Osteoarthritis.
    Shu CC; Jackson MT; Smith MM; Smith SM; Penm S; Lord MS; Whitelock JM; Little CB; Melrose J
    Arthritis Rheumatol; 2016 Apr; 68(4):868-79. PubMed ID: 26636652
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A missense mutation in domain III in HSPG2 in Schwartz-Jampel syndrome compromises secretion of perlecan into the extracellular space.
    Iwata S; Ito M; Nakata T; Noguchi Y; Okuno T; Ohkawara B; Masuda A; Goto T; Adachi M; Osaka H; Nonaka R; Arikawa-Hirasawa E; Ohno K
    Neuromuscul Disord; 2015 Aug; 25(8):667-71. PubMed ID: 26031903
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Spectrum of HSPG2 (Perlecan) mutations in patients with Schwartz-Jampel syndrome.
    Stum M; Davoine CS; Vicart S; Guillot-Noël L; Topaloglu H; Carod-Artal FJ; Kayserili H; Hentati F; Merlini L; Urtizberea JA; Hammouda el-H; Quan PC; Fontaine B; Nicole S
    Hum Mutat; 2006 Nov; 27(11):1082-91. PubMed ID: 16927315
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Perlecan modulates VEGF signaling and is essential for vascularization in endochondral bone formation.
    Ishijima M; Suzuki N; Hozumi K; Matsunobu T; Kosaki K; Kaneko H; Hassell JR; Arikawa-Hirasawa E; Yamada Y
    Matrix Biol; 2012 May; 31(4):234-45. PubMed ID: 22421594
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Structural and functional mutations of the perlecan gene cause Schwartz-Jampel syndrome, with myotonic myopathy and chondrodysplasia.
    Arikawa-Hirasawa E; Le AH; Nishino I; Nonaka I; Ho NC; Francomano CA; Govindraj P; Hassell JR; Devaney JM; Spranger J; Stevenson RE; Iannaccone S; Dalakas MC; Yamada Y
    Am J Hum Genet; 2002 May; 70(5):1368-75. PubMed ID: 11941538
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Perlecan Knockdown Significantly Alters Extracellular Matrix Composition and Organization During Cartilage Development.
    Ocken AR; Ku MM; Kinzer-Ursem TL; Calve S
    Mol Cell Proteomics; 2020 Jul; 19(7):1220-1235. PubMed ID: 32381549
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Perlecan is essential for cartilage and cephalic development.
    Arikawa-Hirasawa E; Watanabe H; Takami H; Hassell JR; Yamada Y
    Nat Genet; 1999 Nov; 23(3):354-8. PubMed ID: 10545953
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Modular Proteoglycan Perlecan/
    Martinez JR; Dhawan A; Farach-Carson MC
    Genes (Basel); 2018 Nov; 9(11):. PubMed ID: 30453502
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Impact of the heparan sulfate proteoglycan perlecan on human disease and health.
    Arikawa-Hirasawa E
    Am J Physiol Cell Physiol; 2022 Jun; 322(6):C1117-C1122. PubMed ID: 35417267
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Matrilysin/MMP-7 Cleavage of Perlecan/HSPG2 Complexed with Semaphorin 3A Supports FAK-Mediated Stromal Invasion by Prostate Cancer Cells.
    Grindel BJ; Martinez JR; Tellman TV; Harrington DA; Zafar H; Nakhleh L; Chung LW; Farach-Carson MC
    Sci Rep; 2018 May; 8(1):7262. PubMed ID: 29740048
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Knockdown of hspg2 is associated with abnormal mandibular joint formation and neural crest cell dysfunction in zebrafish.
    Castellanos BS; Reyes-Nava NG; Quintana AM
    BMC Dev Biol; 2021 Mar; 21(1):7. PubMed ID: 33678174
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Synovial perlecan is required for osteophyte formation in knee osteoarthritis.
    Kaneko H; Ishijima M; Futami I; Tomikawa-Ichikawa N; Kosaki K; Sadatsuki R; Yamada Y; Kurosawa H; Kaneko K; Arikawa-Hirasawa E
    Matrix Biol; 2013 Apr; 32(3-4):178-87. PubMed ID: 23339896
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Evaluation of Human-Induced Pluripotent Stem Cells Derived from a Patient with Schwartz-Jampel Syndrome Revealed Distinct Hyperexcitability in the Skeletal Muscles.
    Yamashita Y; Nakada S; Nakamura K; Sakurai H; Ohno K; Goto T; Mabuchi Y; Akazawa C; Hattori N; Arikawa-Hirasawa E
    Biomedicines; 2023 Mar; 11(3):. PubMed ID: 36979792
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Reduced perlecan in mice results in chondrodysplasia resembling Schwartz-Jampel syndrome.
    Rodgers KD; Sasaki T; Aszodi A; Jacenko O
    Hum Mol Genet; 2007 Mar; 16(5):515-28. PubMed ID: 17213231
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of a novel splice site HSPG2 mutation and prenatal diagnosis in Schwartz Jampel Syndrome type 1 using whole exome sequencing.
    Das Bhowmik A; Dalal A; Matta D; Kandadai RM; Kanikannan MA; Aggarwal S
    Neuromuscul Disord; 2016 Nov; 26(11):809-814. PubMed ID: 27521129
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Perlecan/Hspg2 deficiency alters the pericellular space of the lacunocanalicular system surrounding osteocytic processes in cortical bone.
    Thompson WR; Modla S; Grindel BJ; Czymmek KJ; Kirn-Safran CB; Wang L; Duncan RL; Farach-Carson MC
    J Bone Miner Res; 2011 Mar; 26(3):618-29. PubMed ID: 20814969
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Novel HSPG2 Gene Mutation Causing Schwartz-Jampel Syndrome in a Moroccan Family: A Literature Review.
    Brugnoni R; Marelli D; Iacomino N; Canioni E; Cappelletti C; Maggi L; Ardissone A
    Genes (Basel); 2023 Sep; 14(9):. PubMed ID: 37761893
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.